Visitor Monitoring Drug History: PRED FORTE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: PRED FORTE
FDA Application No: (NDA) 017011
Active Ingredient(s): PREDNISOLONE ACETATE
Company: ALLERGAN
 
Label History
 
Labels are not available on this site for PRED FORTE, (NDA) 017011
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/12/2002 041Control Supplement  
12/4/2001 039Manufacturing Change or Addition  
9/28/2001 038Manufacturing Change or Addition  
7/24/2001 037Manufacturing Change or Addition  
4/12/2001 036Manufacturing Change or Addition  
10/2/2000 035Manufacturing Change or Addition  
5/19/1998 034Control Supplement  
9/30/1997 033Control Supplement  
12/5/1996 032Control Supplement  
5/10/1995 031Control Supplement  
8/3/1995 030Control Supplement  
10/30/1989 029Manufacturing Change or Addition  
10/12/1989 028Manufacturing Change or Addition  
9/9/1988 027Control Supplement  
2/17/1988 026Labeling Revision  
11/3/1987 025Control Supplement  
4/30/1987 024Control Supplement  
6/13/1986 023Control Supplement  
6/13/1986 022Manufacturing Change or Addition  
4/15/1986 021Labeling Revision  
8/13/1982 017Control Supplement  
7/11/1983 016Package Change  
9/3/1982 014Manufacturing Change or Addition  
9/2/1982 013Manufacturing Change or Addition  
1/22/1980 012Manufacturing Change or Addition  
11/19/1979 011Control Supplement  
8/5/1975 003Labeling Revision  
11/26/1974 001Control Supplement  
5/30/1973 000Approval  
 
Therapeutic Equivalents
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